Reported Jun 26, 2013 · Terminated

Philips Diagnost Stationary Radiographic System Models: 712020, 712022, 712050, 712052, 712055, 712057, 712062 Product…

Philips Healthcare Inc.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: Philips Healthcare Inc. · 3000 Minuteman Road · Andover, MA · 01810

Is this the product you have?

  • Philips Diagnost
  • Stationary Radiographic System Models
    • 712020
    • 712022
    • 712050
    • 712052
    • 712055
    • 712057
    • 712062
  • Product UsageUniversal RAD Applications
Lot codes and dates
  • Serial numbers

    101 of 101 codes

    • 316235
    • 335517
    • 321739
    • 334582
    • 359767
    • 357879
    • 344896
    • 351321
    • 356953
    • 365640
    • 365639
    • 359449
    • 363674
    • 375601/SN0802006
    • 368428
    • 7272440
    • 372848
    • 373508
    • 375366
    • 396836/SN0802372
    • 382140/SN0702475
    • 381883/SN0802010
    • 393931/SN0802399
    • 396572/SN0802281
    • 392502/SN0802179
    • 390113/SN0802451
    • 386784/SN0802264
    • 381098/SN0802124
    • 390098/SN0802242
    • 382018/SN0802118
    • 9000529
    • 373499/SN0802249
    • 383639/SN0802099
    • 390129/SN0802521
    • 404296/SN0802460
    • 404298/SN0802474
    • 416255/SN0902004
    • 802119
    • 409788/SN0802635
    • 406492/SN0802489
    • 390393/SN0802337
    • 399024/SN0802562
    • 402837/SN0802410
    • 408716/SN0802551
    • 408239/SN0802583
    • 408240/SN0802630
    • 408236/SN0802554
    • 406024/SN0802481
    • 408591
    • 406156/SN0802537
    • 406140/SN0802479
    • 407675/SN0802517
    • 408967/SN0802547
    • 414087/SN08000100
    • 435757/SN09000361
    • 422092/SN0902023
    • 415783/SN0802662
    • 422536/SN09000199
    • 416904/SN08000052
    • 421962/SN09000054
Amount recalled
101 units

This recall covers 4 products

The agency filed one notice per product. You are reading one of them; the other 3 are below.

Where it was sold

  • Nationwide

Why it was recalled

Installation Acceptance Test Document (IATD) non compliant with regulations. Records shows table height measurements out of specification with the consequence of potential system mis-alignment.

This product could cause temporary or reversible health problems — stop using it.

Want the full recall guide?

The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Notice updated Sep 30, 2016 · Data as of Sep 19, 6:17 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.